List of variants in gene TTN reported as likely benign for Primary dilated cardiomyopathy

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.35264A>C (p.Lys11755Thr)	rs189966800	0.00172
NM_001267550.2(TTN):c.37432C>T (p.Pro12478Ser)	rs200992277	0.00143
NM_001267550.2(TTN):c.79612A>G (p.Thr26538Ala)	rs150682764	0.00100
NM_001267550.2(TTN):c.87412C>A (p.Pro29138Thr)	rs72648227	0.00073
NM_133379.5(TTN):c.16613G>A (p.Arg5538His)	rs145932311	0.00071
NM_001267550.2(TTN):c.50758C>G (p.Pro16920Ala)	rs377289817	0.00064
NM_001267550.2(TTN):c.107576T>C (p.Met35859Thr)	rs72629793	0.00063
NM_001267550.2(TTN):c.39211+6C>T	rs187365142	0.00061
NM_001267550.2(TTN):c.88733G>A (p.Arg29578His)	rs374147064	0.00030
NM_001267550.2(TTN):c.65729T>C (p.Ile21910Thr)	rs146941600	0.00028
NM_001267550.2(TTN):c.38975A>T (p.Lys12992Ile)	rs746094582	0.00019
NM_001267550.2(TTN):c.92699A>G (p.Asn30900Ser)	rs186234393	0.00015
NM_001267550.2(TTN):c.53590A>G (p.Thr17864Ala)	rs375309278	0.00011
NM_001267550.2(TTN):c.107696T>C (p.Ile35899Thr)	rs372276487	0.00006
NM_001267550.2(TTN):c.75034C>T (p.Arg25012Trp)	rs368914555	0.00006
NM_001267550.2(TTN):c.31472T>C (p.Met10491Thr)	rs769226745	0.00004
NM_001267550.2(TTN):c.26765G>A (p.Arg8922Gln)	rs397517520	0.00002
NM_001267550.2(TTN):c.46079T>C (p.Ile15360Thr)	rs1465320800	0.00002
NM_001267550.2(TTN):c.80858C>T (p.Thr26953Met)	rs377506142	0.00002
NM_001267550.2(TTN):c.103540G>A (p.Val34514Ile)	rs769311670	0.00001
NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe)	rs539735520	0.00001
NM_001267550.2(TTN):c.106342C>T (p.Arg35448Trp)	rs530453291	0.00001
NM_001267550.2(TTN):c.27914G>A (p.Arg9305Gln)	rs397517527	0.00001
NM_001267550.2(TTN):c.3011A>C (p.Glu1004Ala)	rs1413214135	0.00001
NM_001267550.2(TTN):c.41282G>A (p.Arg13761His)	rs781139091	0.00001
NM_001267550.2(TTN):c.47495G>A (p.Arg15832Gln)	rs376140223	0.00001
NM_001267550.2(TTN):c.50999G>A (p.Arg17000Lys)	rs767481574	0.00001
NM_001267550.2(TTN):c.71881G>A (p.Val23961Ile)	rs397517690	0.00001
NM_001267550.2(TTN):c.74527A>G (p.Asn24843Asp)	rs373527654	0.00001
NM_001267550.2(TTN):c.37502C>T (p.Pro12501Leu)	rs1236045684
NM_001267550.2(TTN):c.63571C>A (p.Pro21191Thr)	rs2049345864
NM_001267550.2(TTN):c.74468C>G (p.Ala24823Gly)	rs368071644
NM_001267550.2(TTN):c.97760G>C (p.Arg32587Pro)	rs55704830

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